2X3W
structure of mouse syndapin I (crystal form 2)
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | BESSY BEAMLINE 14.1 |
Synchrotron site | BESSY |
Beamline | 14.1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2009-10-02 |
Detector | MARMOSAIC 225 mm CCD |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 88.280, 154.610, 191.740 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 34.360 - 2.640 |
R-factor | 0.22335 |
Rwork | 0.221 |
R-free | 0.27373 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.006 |
RMSD bond angle | 0.850 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHASER |
Refinement software | REFMAC (5.3.0040) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 34.350 | 2.750 |
High resolution limit [Å] | 2.640 | 2.640 |
Rmerge | 0.130 | 0.690 |
Number of reflections | 38766 | |
<I/σ(I)> | 10.81 | 2.88 |
Completeness [%] | 99.7 | 99.1 |
Redundancy | 7.17 | 7.03 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 5.3 | 2.5UL SYNDAPIN(5MG/ML IN 50MM HEPES, 50MM NACL) MIXED WITH 0.5UL 0.3M GLYCYL-GLYCYL-GLYCINE AND 2UL WELL SOLUTION 0.1M NAAC/HAC PH5.0, 3%(W/V) PEG4000., pH 5.3 |